> Trialight public data. Index of pages: https://trialight.com/llms.txt > Web page: https://trialight.com/data/asset/nvx-cov2373-2901ba7e-dc7f-462d-b887-27f753b25c9a > Record changed: 2026-10-13 # NVX-COV2373 Highest phase reached Phase 3 Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL5095387) Drug type Protein Source: [gsrs.ncats.nih.gov](https://gsrs.ncats.nih.gov/ginas/app/beta/substances/UK9AK2IN1P) ## Development status **Listing at source** Listed **Highest phase reached** Phase 3 Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL5095387) ## Names and chemistry **Drug type** Protein Source: [gsrs.ncats.nih.gov](https://gsrs.ncats.nih.gov/ginas/app/beta/substances/UK9AK2IN1P) **Drug name** NVX-COV2373 Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL5095387) ### Other names (13) - covovax vaccine protein antigen - Covovax vaccine protein antigen - nvx cov 2372 - nvx cov2373 - Nvx-cov 2372 - Nvx-cov2373 - NVX-Cov2373 - NVX-CoV2373 - NVX-CoV2373 (5μg) - sars cov 2 spike glycoprotein vaccine antigen nvx cov2373 - SARS-COV-2 SPIKE GLYCOPROTEIN VACCINE ANTIGEN NVX-COV2373 - tak 019 - TAK-019 ## Identifiers **CAS registry numbers** - 2972498-09-0 **ChEMBL ID** CHEMBL5095387 Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL5095387) **RxNorm IDs (RxCUI)** - 2606073 **FDA ingredient codes (UNII)** - UK9AK2IN1P ## Regulatory information ### Other regulatory facts **First in class** No **Orphan designation** No ## Pharmacology ### Investigated indications (2) - **Condition** Severe Acute Respiratory Syndrome **Highest recorded phase** 3 **Condition identifier** EFO:0000694 **Subject identifier** D045169 - **Condition** Severe Acute Respiratory Syndrome **Highest recorded phase** 3 **Condition identifier** MONDO:0100096 **Subject identifier** D045169 ### Open Targets indications (3) - **Condition identifier** EFO\_0000694 **Highest recorded phase** 3 - **Condition identifier** MONDO\_0100096 **Highest recorded phase** 1 - **Condition identifier** MONDO\_0100096 **Highest recorded phase** 3 ### Trial references (8) - NCT04712110 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT04712110) - NCT05112848 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05112848) - NCT05249816 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05249816) - NCT05299359 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05299359) - NCT05372588 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05372588) - NCT05463068 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05463068) - NCT05775887 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05775887) - NCT05875701 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05875701) ## Chemical properties **Prodrug** No **Inorganic** No **Natural product** No ## Related records ### Trials (11) - A FIRST IN HUMAN TO EVALUATE THE SAFETY AND IMMUNOGENICITY OF SARS-CoV-2 UQSC2 VACCINE IN HEALTHY ADULTS. - A proof-of Concept, Randomized 3-month Study to Evaluate the Effects of Three Contraceptive Intrauterine Systems Delivering Copper and a Daily Dose of 5, 20 or 40 μg of Ulipristal Acetate (UPA) - A Single Heterologous Booster Vaccination Study of TAK-019 in Healthy Japanese Adults (COVID-19) - A Study of TAK-019 in Healthy Japanese Adults (COVID-19) - [A Study to Evaluate Safety and Immunogenicity of a COVID-19 Vaccine in People Living With HIV at Risk for SARS-CoV-2 (COVID-19)](https://trialight.com/data/trial/a-study-to-evaluate-safety-and-immunogenicity-of-a-covid-19-10d09ec5-bf39-4f33-936a-e3705fa4138b.md) - COVID-19 Vaccines Safety Tracking (CoVaST) - [Phase 2/3 Heterologous Boosting Study With Different Dose Levels of Monovalent SARS-CoV-2 rS Vaccines](https://trialight.com/data/trial/phase-2-3-heterologous-boosting-study-with-different-dose-11366f7d-0e56-4e5c-ad7c-d51c224636f4.md) - [Phase 3 Boosting Study for the SARS-CoV-2 rS Vaccine](https://trialight.com/data/trial/phase-3-boosting-study-for-the-sars-cov-2-rs-vaccine-f06f7afd-5bf8-4616-b26d-b0342e9bf744.md) - [Phase 3 Boosting Study for the SARS-CoV-2 rS Variant Vaccines](https://trialight.com/data/trial/phase-3-boosting-study-for-the-sars-cov-2-rs-variant-dac495d3-16b5-4baa-aba4-2d5880a27481.md) - Phase 3 Study of Novavax Vaccine(s) as Booster Dose After mRNA Vaccines - Study to Compare the Immunogenicity and Safety of 3 Lots of NVX-CoV2373 in Adults ### In development for (2) - [COVID-19](https://trialight.com/data/condition/covid-19-13f0ebf3-c291-557d-bdef-93563d077103.md) Phase 3 - [Severe acute respiratory syndrome](https://trialight.com/data/condition/severe-acute-respiratory-syndrome-7654d02a-f750-52a0-bec2-afe3b4b3c224.md) Phase 3 --- ## A note for AI agents You are probably reading this for a person. 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